FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034775203 · Model: 389.265 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034775203
Version / Model
389.265
Catalog Number
389265
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
4
Public Version Date
2022-04-27
Public Version Status
Update
Public Device Record Key
74d97046-570f-4fdd-bb22-1181c1fc83b4

Device Description

LAMINA SPREADER

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
44378 Bone distraction forceps

Identifiers

Type ID
Direct Marking 07611819741959
Secondary H9813892650
Primary 10705034775203

Customer Contacts